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Protein Coding Gene : Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1

Primary Identifier  MGI:105083 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  20510
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables amino acid transmembrane transporter activity; identical protein binding activity; and monoatomic anion channel activity. Involved in several processes, including learning or memory; modulation of chemical synaptic transmission; and response to alkaloid. Acts upstream of or within several processes, including behavioral fear response; cellular response to bisphenol A; and cellular response to mercury ion. Located in endosome membrane; membrane raft; and plasma membrane. Is active in several cellular components, including Schaffer collateral - CA1 synapse; apical plasma membrane; and recycling endosome. Is expressed in several structures, including alimentary system; eye; genitourinary system; hemolymphoid system gland; and nervous system. Used to study dicarboxylic aminoaciduria and low tension glaucoma. Human ortholog(s) of this gene implicated in dicarboxylic aminoaciduria and schizophrenia 18. Orthologous to human SLC1A1 (solute carrier family 1 member 1).
PHENOTYPE: Mice homozygous for disruptions in this gene display reduced locomotor activity and excessive excretion of glutamate and aspartate. [provided by MGI curators]
  • synonyms:
  • MEAAC1,
  • MGI:2441941,
  • RIKEN cDNA D130048G10 gene,
  • EAAC1,
  • solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1,
  • Slc1a1,
  • MGD-MRK-32123,
  • D130048G10Rik,
  • EAAT3

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

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Proteins

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Function

Mouse features --> Functions (GO terms)

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